[rare pigmentary atrophic autosomal recessive disease manifested as an extreme photosensitivity to ultraviolet light as the result of a deficiency in the enzyme that permits excisional repair of utraviolet damaged DNA. ( CSP )]
UMLS (NCI) C0043346 Relation/PAR: Genetic Condition
Photodermatitis
Precancerous Condition
Congenital anomalies of the integument
Pigmentation Disorders